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Neonates With SARS-CoV-2 Infection and Pulmonary Disease Safely Treated With Remdesivir
Bedangshu Saikia1, Julian Tang2, Simon Robinson1
1From the Paediatric Intensive Care, Leicester Children's Hospital, Leicester, United Kingdom.
Insights
Two premature infants with severe SARS-CoV-2 pulmonary disease, presenting with apnea, were successfully treated with remdesivir (RDV). This highlights RDV
Area of Science:
- Neonatology
- Pediatric Infectious Diseases
- Pulmonology
Background:
- Premature infants are a high-risk group for severe outcomes from SARS-CoV-2 infection.
- Respiratory distress and apnea are potential early symptoms in neonates with SARS-CoV-2.
Observation:
- Two extremely premature infants presented with recurrent apnea and progressed to severe SARS-CoV-2-related pulmonary disease requiring mechanical ventilation.
- Both infants received compassionate use of remdesivir (RDV) for treatment.
Findings:
- Successful treatment of severe SARS-CoV-2 pulmonary disease in two neonates using remdesivir (RDV).
- No adverse side effects were observed during RDV treatment in these high-risk infants.
- Early recognition of potential deterioration and multidisciplinary team involvement are crucial for timely intervention.
Implications:
- SARS-CoV-2 infection can manifest as apnea and progress to severe pulmonary disease in neonates.
- Remdesivir (RDV) appears to be a safe and effective treatment option for severe SARS-CoV-2 in this population.
- Experience informs the development of guidelines for RDV use in children under 12, especially infants.
Abstract:
We describe 2 expremature infants presenting with SARS-CoV-2-related pulmonary disease in their second and fifth week of life needing support with mechanical ventilation. Both infants' initial presentation was with repeated apneas. These cases highlight that SARS-CoV-2 infection could present with apneas and has the potential to progress to more severe pulmonary disease in this high-risk age group of patients. Both patients were treated with remdesivir (RDV). We provide the data of 2 high-risk neonates successfully treated with RDV without observation of any described side effects. A recognition that these high-risk neonates could deteriorate and early multidisciplinary team discussion is the mainstay to the compassionate access to RDV. Our experience led us to develop a guideline on the use of RDV below 12 years of age, with particular focus on infants and young children.
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